A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351278



Internal ID21008831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206257442..206259705hg38UCSC Ensembl
chr2:207122166..207124429hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg382264
hg192264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082953
Samples
Known GenesGPR1-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351278
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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